Linked Data
dbSNP Id:
rs189446113
gnomAD v4:
11-123058942-A-T
MyVariant Identifiers:
chr11:g.122929650A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.123058942A>T , CM000673.2:g.123058942A>T | GRCh38 |
| NC_000011.9:g.122929650A>T , CM000673.1:g.122929650A>T | GRCh37 |
| NC_000011.8:g.122434860A>T | NCBI36 |
| NG_029473.1:g.8195T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000534624.6:c.1324-112T>A (HSPA8) MANE Select | ENSP00000432083.1:n.1324-112T>A | |
| ENST00000227378.7:c.1324-112T>A (HSPA8) | ENSP00000227378.3:n.1324-112T>A | |
| ENST00000453788.6:c.1324-112T>A (HSPA8) | ENSP00000404372.2:n.1324-112T>A | |
| ENST00000524552.5:c.97-112T>A (HSPA8) | ENSP00000435908.1:n.97-112T>A | |
| ENST00000526110.5:c.1267-112T>A (HSPA8) | ENSP00000433584.1:n.1267-112T>A | |
| ENST00000526686.1:c.-133T>A (HSPA8) | ENSP00000435019.1:n.-133T>A | |
| ENST00000532091.1:n.1187T>A (HSPA8) | ||
| ENST00000532636.5:c.1324-112T>A (HSPA8) | ENSP00000437125.1:n.1324-112T>A | |
| ENST00000533238.5:n.426-112T>A (HSPA8) | ||
| ENST00000533540.5:c.886-112T>A (HSPA8) | ENSP00000437189.1:n.886-112T>A | |
| ENST00000534319.5:c.616-112T>A (HSPA8) | ENSP00000433316.1:n.616-112T>A | |
| ENST00000534624.5:c.1324-112T>A (HSPA8) | ENSP00000432083.1:n.1324-112T>A | |
| NM_006597.5:c.1324-112T>A (HSPA8) | NP_006588.1:n.1324-112T>A | |
| NM_153201.3:c.1324-112T>A (HSPA8) | NP_694881.1:n.1324-112T>A | |
| NR_001454.2:n.54T>A (SNORD14D) | ||
| XM_011542798.1:c.1324-112T>A (HSPA8) | XP_011541100.1:n.1324-112T>A | |
| NM_006597.6:c.1324-112T>A (HSPA8) MANE Select | NP_006588.1:n.1324-112T>A | |
| NM_153201.4:c.1324-112T>A (HSPA8) | NP_694881.1:n.1324-112T>A |